Apply for Medtronic Hiring Clinical Studies Support Coordinator II Mumbai. Remote full-time role with clinical data coordination responsibilities.
About the Company
Medtronic is a global leader in healthcare technology, dedicated to improving patient outcomes and expanding access to life-saving therapies across the world. With decades of innovation and a strong ethical foundation, Medtronic operates in more than 150 countries and touches millions of lives every year through medical devices, diagnostics, and digital health solutions.
At Medtronic, employees are encouraged to lead with purpose and compassion. The organization believes that innovation thrives in inclusive environments where diverse ideas are welcomed and nurtured. Medtronic’s mission-driven culture focuses on breaking down barriers to healthcare access and equity while empowering employees to build meaningful, long-term careers. Hiring Clinical Studies Support Coordinator II
Working at Medtronic means being part of a connected global team that values integrity, collaboration, and continuous improvement. Employees are supported through competitive compensation, flexible benefits, and opportunities to grow across functions and geographies. Hiring Clinical Studies Support Coordinator II
Job Details
- Job Title: Clinical Studies Support Coordinator II
- Job Requisition ID: R57540
- Job Type: Full-Time
- Work Mode: Remote
- Job Category: Clinical Operations / Clinical Support
- Location: Mumbai, Maharashtra, India
- Posting Status: Posted Today
- Career Stream: Office Support
This role is ideal for professionals with prior clinical data or document coordination experience who are looking to grow within a global medical technology organization.
Job Description
The Clinical Studies Support Coordinator II plays a critical role in supporting clinical studies through effective coordination of data, documentation, and administrative activities. This position contributes directly to the successful execution of clinical studies by ensuring accuracy, completeness, and compliance of clinical data and study files. Hiring Clinical Studies Support Coordinator II
The role involves close collaboration with clinical operations teams, internal stakeholders, and study personnel to maintain high-quality study documentation and resolve data discrepancies. As an established individual contributor, the coordinator works under moderate supervision while applying prior experience to routine and semi-routine clinical support tasks.
This position provides strong exposure to clinical research processes, study databases, audits, and compliance requirements, making it a valuable career step for professionals in clinical research support or clinical operations. Hiring Clinical Studies Support Coordinator II
Key Responsibilities
- Support clinical studies by executing and maintaining assigned clinical support activities
- Actively participate in the development, testing, and maintenance of case report forms (CRFs), study reports, and clinical study databases
- Ensure timely and accurate completion of clinical data forms in accordance with study protocols
- Verify study data and identify, manage, and resolve data discrepancies
- Generate and track data queries to ensure data quality and integrity
- Process study-related compensation activities and identify discrepancies when applicable
- Create, organize, and maintain clinical study files in compliance with internal procedures
- Manage the organization, control, and distribution of clinical study documents
- Assist with periodic internal audits of clinical study files to ensure completeness and accuracy
- Highlight areas of concern or process gaps and suggest practical solutions within assigned responsibilities
- Provide guidance and assistance to new or entry-level team members as needed
Hiring Clinical Studies Support Coordinator II
Skills and Qualifications
Educational Background
- Bachelor’s degree in Life Sciences, Pharmacy, Clinical Research, or a related discipline preferred
Required Experience
- Minimum of 2 years of relevant experience in clinical studies support, clinical data coordination, or clinical documentation
- Prior exposure to clinical trial processes, study databases, or clinical research environments
Technical Skills
- Knowledge of clinical study documentation and data management processes
- Familiarity with case report forms, clinical databases, and study protocols
- Understanding of basic clinical audit and compliance requirements
- Proficiency in standard office tools and clinical documentation systems
Soft Skills
- Strong attention to detail and accuracy
- Ability to manage routine tasks with consistency and reliability
- Good organizational and time-management skills
- Effective written and verbal communication abilities
- Capability to work independently under moderate supervision
- Willingness to identify issues and contribute to process improvements
Hiring Clinical Studies Support Coordinator II
Benefits and Perks
- Competitive salary aligned with industry standards
- Flexible benefits package designed to support work-life balance
- Eligibility for the Medtronic Incentive Plan (MIP), a short-term incentive program
- Remote working flexibility
- Access to professional development resources and learning opportunities
- Inclusive and purpose-driven work culture
- Supportive environment focused on employee wellbeing and growth
Hiring Clinical Studies Support Coordinator II
Why You Should Join Medtronic
Medtronic offers more than just a job; it offers a meaningful career built around improving lives. As a Clinical Studies Support Coordinator II, you will contribute directly to clinical research efforts that help bring innovative medical technologies to patients worldwide. Hiring Clinical Studies Support Coordinator II
This role provides an excellent opportunity to strengthen your experience in clinical data coordination, documentation management, and audit readiness while working remotely with global teams. Medtronic’s emphasis on ethics, quality, and innovation ensures that employees gain exposure to best-in-class clinical practices.
For professionals seeking stability, growth, and purpose in their careers, Medtronic provides a platform to learn, contribute, and advance within the healthcare technology space. Hiring Clinical Studies Support Coordinator II
FAQs
Is this a remote position?
Yes, this is a fully remote role based in Mumbai, Maharashtra, India.
What experience is required for this role?
A minimum of 2 years of relevant experience in clinical studies support or related areas is required.
Does this role involve clinical data handling?
Yes, the role includes data coordination, data verification, and discrepancy management.
Is this an entry-level position?
No, this is an experienced support role designed for established individual contributors.
Are incentives included in the compensation?
Yes, this position is eligible for the Medtronic Incentive Plan (MIP).
How to Apply
Interested candidates should apply through the official Medtronic careers portal by searching for Job Requisition ID R57540 – Clinical Studies Support Coordinator II. Complete the online application with accurate professional and educational details to be considered for this role.
Early applications are encouraged due to high demand for remote clinical roles. Hiring Clinical Studies Support Coordinator II
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